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1.
Accumulation of Carbamylation-Derived Products in Aneurysmal Aorta.
J Vasc Res
; 61(2): 51-58, 2024.
Article
in English
| MEDLINE | ID: mdl-38246153
2.
Pediatric ANCA vasculitis: clinical presentation, treatment, and outcomes in a French retrospective study.
Pediatr Nephrol
; 38(8): 2649-2658, 2023 08.
Article
in English
| MEDLINE | ID: mdl-36622443
3.
To biopsy or not to biopsy: Henoch-Schönlein nephritis in children, a 5-year follow-up study.
Pediatr Nephrol
; 37(1): 147-152, 2022 01.
Article
in English
| MEDLINE | ID: mdl-34224002
4.
Carbamylated Proteins in Renal Disease: Aggravating Factors or Just Biomarkers?
Int J Mol Sci
; 23(1)2022 Jan 05.
Article
in English
| MEDLINE | ID: mdl-35008998
5.
Amniotic fluid peptides predict postnatal kidney survival in developmental kidney disease.
Kidney Int
; 99(3): 737-749, 2021 03.
Article
in English
| MEDLINE | ID: mdl-32750455
6.
Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice.
Am J Hum Genet
; 101(5): 803-814, 2017 Nov 02.
Article
in English
| MEDLINE | ID: mdl-29100091
7.
Treatment and outcome of congenital nephrotic syndrome.
Nephrol Dial Transplant
; 34(3): 458-467, 2019 03 01.
Article
in English
| MEDLINE | ID: mdl-29474669
8.
Protein carbamylation is a hallmark of aging.
Proc Natl Acad Sci U S A
; 113(5): 1191-6, 2016 Feb 02.
Article
in English
| MEDLINE | ID: mdl-26712018
9.
Eculizumab treatment in severe pediatric STEC-HUS: a multicenter retrospective study.
Pediatr Nephrol
; 33(8): 1385-1394, 2018 08.
Article
in English
| MEDLINE | ID: mdl-29572749
10.
Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome.
Pediatr Nephrol
; 33(3): 473-483, 2018 03.
Article
in English
| MEDLINE | ID: mdl-29058154
11.
Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract.
J Am Soc Nephrol
; 28(10): 2901-2914, 2017 Oct.
Article
in English
| MEDLINE | ID: mdl-28566479
12.
C5 nephritic factors drive the biological phenotype of C3 glomerulopathies.
Kidney Int
; 92(5): 1232-1241, 2017 11.
Article
in English
| MEDLINE | ID: mdl-28712854
13.
Mutations of CEP83 cause infantile nephronophthisis and intellectual disability.
Am J Hum Genet
; 94(6): 905-14, 2014 Jun 05.
Article
in English
| MEDLINE | ID: mdl-24882706
14.
Signaling of Serum Amyloid A Through Receptor for Advanced Glycation End Products as a Possible Mechanism for Uremia-Related Atherosclerosis.
Arterioscler Thromb Vasc Biol
; 36(5): 800-9, 2016 05.
Article
in English
| MEDLINE | ID: mdl-26988587
15.
Infection-related hospitalizations after kidney transplantation in children: incidence, risk factors, and cost.
Pediatr Nephrol
; 32(12): 2331-2341, 2017 Dec.
Article
in English
| MEDLINE | ID: mdl-28744628
16.
Homocitrulline: a new marker for differentiating acute from chronic renal failure.
Clin Chem Lab Med
; 54(1): 73-9, 2016 Jan.
Article
in English
| MEDLINE | ID: mdl-26124058
17.
Reconsidering the Lack of Urea Toxicity in Dialysis Patients.
Semin Dial
; 29(5): 333-7, 2016 09.
Article
in English
| MEDLINE | ID: mdl-27174444
18.
Mainzer-Saldino syndrome is a ciliopathy caused by IFT140 mutations.
Am J Hum Genet
; 90(5): 864-70, 2012 May 04.
Article
in English
| MEDLINE | ID: mdl-22503633
19.
A pure familial 6q15q21 split duplication associated with obesity and transmitted with partial reduction.
Am J Med Genet A
; 167(6): 1275-84, 2015 Jun.
Article
in English
| MEDLINE | ID: mdl-25900228
20.
Clinical characteristics and outcomes of childhood-onset ANCA-associated vasculitis: a French nationwide study.
Nephrol Dial Transplant
; 30 Suppl 1: i104-12, 2015 Apr.
Article
in English
| MEDLINE | ID: mdl-25676121